Atlas FDA

Activa™ Deep Brain Stimulation Therapy System, Percept PC/RC BrainSense™

FDA premarket approval P960009/S524 · decided 2025-12-08

Approval details

PMA number
P960009
Supplement
S524
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
Activa™ Deep Brain Stimulation Therapy System, Percept PC/RC BrainSense™
Generic name
Stimulator, electrical, implanted, for parkinsonian tremor
Applicant
Medtronic, Inc.
Date received
2025-09-29
Decision date
2025-12-08
Days to decision
70 days
Decision code
APPR
Product code
MHY
Advisory committee
Neurology
Expedited review
No
Location
Minneapolis, MN
Statement
approval for updates to the Model A610 Deep Brain Stimulation Clinician Programmer Application version 5.0, which updates background loading of event logs, user interface revisions, and bug fix revisions.

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